Methyl N-(2-fluorophenyl)carbamate

Base Information

Chemical Name:Methyl N-(2-fluorophenyl)carbamate
CAS No.:16664-12-3
Molecular Formula:C8H8FNO2
Molecular Weight:169.155
Hs Code.:
DSSTox Substance ID:DTXSID00392917
Nikkaji Number:J1.604.651E
Wikidata:Q82191431
Mol file:16664-12-3.mol

Synonyms:16664-12-3;methyl (2-fluorophenyl)carbamate;2-fluoro-N-methoxycarbonylaniline;Methyl N-(2-fluorophenyl)carbamate;SCHEMBL513736;DTXSID00392917;2-Fluorophenylcarbamic acid methyl;STK413421;AKOS003286016;2-Fluorophenylamine, N-methoxycarbonyl-;CS-0336921;F3035-0729

Suppliers and Price of Methyl N-(2-fluorophenyl)carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of Methyl N-(2-fluorophenyl)carbamate

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:169.05390666
Heavy Atom Count:12
Complexity:163

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)NC1=CC=CC=C1F

Technology Process of Methyl N-(2-fluorophenyl)carbamate

There total 3 articles about Methyl N-(2-fluorophenyl)carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%

: 67-56-1
methanol

: 445-28-3
2-fluorobenzamide

: 16664-12-3
methyl (2-fluorophenyl)carbamate

Guidance literature:: With sodium bromide; In acetonitrile; at 50 ℃; for 6h; Electrochemical reaction; Green chemistry;
DOI:10.1039/c8ob01059e

Reference yield: 87.0%

: 67-56-1
methanol

: 2597-44-6
formyl radical

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 16664-12-3
methyl (2-fluorophenyl)carbamate

Guidance literature:: With 1,10-Phenanthroline; [trihexyl(tetradecyl)phosphonium hexafluorophosphate]; palladium dichloride; at 135 ℃; for 24h; under 10343.2 Torr;
DOI:10.1021/ol802096x